painless gastroscopy
Conditions
Interventions
Experimental group:The experimental group was given tramadol and sufentanil combined with propofol
control group:The control group was given sufentanil combined with propofol
Sponsors
Xianyang first People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: (1) Painless gastroscopy was to be performed in the outpatient department; (2) Young and middle-aged patients (aged 18-45 years); (3) According to the American Society of Anesthesiologists anesthesia Risk assessment table, assess qualified candidates (ASAI ~ Level II); (4) Approved by the Ethics Committee and informed consent of the patient.
Exclusion criteria
Exclusion criteria: (1) Patients with acute respiratory infections, asthma attacks, respiratory failure and other severe respiratory diseases; (2) Patients with uncontrolled malignant hypertension, unstable angina pectoris, myocardial infarction, malignant arrhythmia and other serious cardiovascular and cerebrovascular diseases; (3) Patients with acute upper gastrointestinal bleeding with shock, gastrointestinal obstruction with gastric content retention, etc., easy to cause reflux, aspiration and asphyxia; (4) Patients in a critical state such as shock or extremely weak, cachexia, etc., who cannot be examined; (5) Patients with severe anemia; (6) Patients with serious other systemic diseases; (7) There is coagulation or immune dysfunction (8) pregnancy and breastfeeding women. (9) There is coagulation or immune dysfunction; (10) Patients with opioid addiction or mental illness (11) are allergic to the drugs used in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anesthetic effect ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean arterial pressure;Propofol dose ;Adverse events;Heart rate; | — |
Countries
China
Contacts
Public ContactQi Mao
Xianyang first People's Hospital
Outcome results
None listed